137171-51-8

Basic information

• Product Name: 2,4,6-tris(4-methoxyphenyl)-2,4,6-trisulfanylene-1,3,5,2,4,6-trioxatriphosphinane
• CAS NO: 137171-51-8
• Molecular Weight: 558.513
• Mol File: 137171-51-8.mol
• Article Data: 15

Chemical Properties

• CAS DataBase Reference: 2,4,6-tris(4-methoxyphenyl)-2,4,6-trisulfanylene-1,3,5,2,4,6-trioxatriphosphinane(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4,6-tris(4-methoxyphenyl)-2,4,6-trisulfanylene-1,3,5,2,4,6-trioxatriphosphinane(137171-51-8)
• EPA Substance Registry System: 2,4,6-tris(4-methoxyphenyl)-2,4,6-trisulfanylene-1,3,5,2,4,6-trioxatriphosphinane(137171-51-8)

Safety Data

• Hazardous Substances Data: 137171-51-8(Hazardous Substances Data)

Upstream product

• 923-99-9 tri-n-propyl phosphite 
• 19172-47-5 Lawessons reagent 
• 57-57-8 β-Propiolactone 
• 1457-47-2 3-allylrhodanine 
• 54262-97-4 2,2,6,6-tetramethylpiperidine-1-carboxaldehyde 
• 1989-32-8 2-fluoren-9-ylidene-malononitrile 
• 6048-49-3 xanthen-9-ylidene-malononitrile 
• 1499-21-4 Diphenylphosphinic chloride 
• 1706-90-7 methyl diphenylphosphinate 
• 495-71-6 phenacylacetophenone 
• 5651-50-3 2-methyl-4H-benzo[d][1,3]oxathiin-4-one 
• 116-17-6 triisopropyl phosphite 
• 5651-35-4 2-phenylbenzo[d]-1,3-oxathiin-4-one 
• 78120-45-3 (Z)-3-Thiobenzoylamino-but-2-enoic acid ethyl ester 

Downstream Products

• 851363-75-2 O-methyl hydrogen (4-methoxyphenyl)phosphonothioate 
• 858128-22-0 O,O-dimethyl (4-methoxyphenyl)phosphonothioate 
• 858128-33-3 (4-methoxyphenyl)phosphonothioic O,O'-acid 
• 858128-24-2 O-methyl (4-methoxyphenyl)phosphonochloridothioate 
• 858128-29-7 O-methyl (4-methoxyphenyl)phosphonothioic O,O-anhydride 

Relevant articles and documents

The behaviour of Lawesson's reagent and dialkylaminophosphines towards dicyanomethylene derivatives of xanthone and fluorenone

Lawesson's reagent 1 reacts with xanthen-9-ylidenemalono-nitrile 3 to give adducts 5a, 6a and 7, respectively. In case of the reaction of fluoren-9-ylidenemalononitrile 4 with 1, only 3-amino-2-fluoren-9-ylidene-3- thioxopropanenitrile 5b is obtained toge

Reactions of nitroxides with sulfur-containing compounds, part IV: Synthesis of novel nitroxide (thio)ureas

The reactions of 4-isothiocyanato-2,2, 6,6-tetramethylpiperidine-1-oxyl 2 and 4-isocyanato-2,2,6,6-tetramethylpiperidine-1-oxyl 3 with selected amines and lower alcohols give the corresponding novel thioureas 4, ureas 5, thiocarbamates 6, and carbamates 7, all bearing the nitroxyl moiety. The characteristic features of EI mass spectra of (thio)ureas 4 and 5 are described. Some of the synthesized thioureas 4, ureas 5, thiocarbamates 6, and carbamates 7 are moderately or weakly active against pathogenic fungi.

THE BEHAVIOUR OF p-QUINONEDIIMINES TOWARDS 2,4-BIS-(4-METHOXYPHENYL)-1,3,2,4-DITHIADIPHOSPHETANE-2,4-DISULFIDE

p-Benzoquinonediimines (IIIa-c) react with 2,4-bis-(4-methoxyphenyl)-1,3,2,4-dithiadiphosphetane-2,4-disulfide (I) to produce compounds Va-c. p-Naphthoquinonediimines (IVa,b) react with the same reagent to produce compounds Xa,b. Key words: p-Benzoquinonedibenzenesulfonimine IIIa; p-benzoquinonedimethanesulfonimine IIIb; p-benzoquinonedibenzimide IIIc; 1,4-naphthoquinonedibenzenesulfonimine IVa; 1,4-naphthoquinonedimethanesulfonimine IVb; 2,4-bis-(4-methoxyphenyl)-1,3,2,4-dithiadiphosphetane-2,4-disulfide (Lawesson Reagent) I; 1,3,2-benzoazathiaphophole-2-sulfides (V); 1,3,2-naphthoazathiaphophole-2-sulfides X).